Canonical Allele Identifier: CA9886215

Gene: ZNF335

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45971280G>C , CM000682.2:g.45971280G>C	GRCh38
NC_000020.10:g.44599919G>C , CM000682.1:g.44599919G>C	GRCh37
NC_000020.9:g.44033326G>C	NCBI36
NG_029772.1:g.5915C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022095.4:c.131C>G MANE Select	NP_071378.1:p.Ala44Gly
ENST00000322927.3:c.131C>G MANE Select	ENSP00000325326.2:p.Ala44Gly
NM_022095.3:c.131C>G	NP_071378.1:p.Ala44Gly
ENST00000322927.2:c.131C>G	ENSP00000325326.2:p.Ala44Gly
XM_005260504.3:c.131C>G	XP_005260561.1:p.Ala44Gly
XM_005260504.4:c.131C>G	XP_005260561.1:p.Ala44Gly
XM_005260506.2:c.-157C>G	XP_005260563.1:n.-157C>G
XM_011528979.1:c.131C>G	XP_011527281.1:p.Ala44Gly
XM_011528979.3:c.131C>G	XP_011527281.1:p.Ala44Gly
XM_017028012.1:c.-157C>G	XP_016883501.1:n.-157C>G
XR_001754372.2:n.622C>G
XR_002958500.1:n.622C>G
XR_002958501.1:n.622C>G
XR_936602.1:n.642C>G
XR_936602.3:n.622C>G
XR_936603.1:n.643C>G
XR_936604.1:n.643C>G
XR_936604.3:n.622C>G